Papers ( 2013 – 2018 )

2018

  1. Doungmanee, S.; Siritanon, T.; Insuwan, W.; Jungsuttiwong, S.; Rangsriwatananon, K. Multi step energy transfer between three Si_LTL and SiGe_LTL zeoliteloaded dyes, Journal of Porous Materials, 2018, 1381–1389.
  2. Mudchimo, T.; Namuangruk, S.; Kungwan, N. and Jungsuttiwong, S. Carbon-Doped Boron Nitride Nanosheet as a Promising Metal-Free Catalyst for NO Reduction: DFT mechanistic study, Applied Catalysis A: General, 2018, 557, 79–88.
  3. Wongnongwa, Y.; Namuangruk, S.; Kungwan, N.; and Jungsuttiwong, S. Catalytic reduction mechanism of deoxygenation of NO via the CO-reaction pathway using nanoalloy Ag7Au6 clusters: density functional theory investigation, New Journal of Chemistry, 2018, 42, 14120–14127
  4. Yodsin, N.; Rungnim, C.; Promarak, V.; Namuangruk, S.; Kungwan, N.; Rattanawan, R.; and Jungsuttiwong, S. Influence of Hydrogen Spillover on Pt-Decorated Carbon Nanocones for Enhancing Hydrogen Storage Capacity: DFT Mechanistic Study, Physical Chemistry Chemical Physics, 2018, 20, 21194-21203

2017

  1. Hadsadee, S.; Rattanawan, R.; Tarsang, R.; Kungwan, N.; Jungsuttiwong, S. Push-Pull N-Annulated Perylene-Based Sensitizers for Dye-Sensitized Solar Cells: Theoretical Property Tuning by DFT/TDDFT, ChemistrySelect, 2017, 2, 9829– 9837.
  2. Jungsuttiwong, S.; Sirithip, K.; Prachumrak, N.; Tarsang, R.; Sudyoadsuk, T.; Namuangruk, S.; Kungwan, N.; Promarak, V.; Keawin, T. Significant enhancement in the performance of porphyrin for dye-sensitized solar cells: aggregation control using chenodeoxycholic acid, New Journal of Chemistry, 2017, 41, 7081-7091.
  3. Wongnongwa,Y.; Namuangruk, S.; Kungwan, N.; Jungsuttiwong, S. Mechanistic study of CO oxidation by N2O over Ag7Au6 cluster investigated by DFT methods, Applied Catalysis A: General, 2017, 538, 99-106.
  4. Liu, H.; Lou, Y.; Jungsuttiwong, S.; Yuan, S.; Zhao, Y.; Wang, Z.; Shi, L. and Zhou, H. Fence Constructed at a Semiconductor/Electrolyte Interface Improving the Electron Collection Efficiency of the Photoelectrode for a Dye-Sensitized Solar Cell, ACS Applied Materials & Interfaces, 2017, 9, 2396−2402.
  5. Keawin, T.; Tarsang, R.; Sirithip, K.; Prachumrak, N.; Sudyoadsuk, T.; Namuangruk, S.; Roncali, J.; Kungwan, N.; Promarak, V.; Jungsuttiwong, S. Anchoring number-performance relationship of zinc-porphyrin sensitizers for dye-sensitized solar cells: A combined experimental and theoretical study, Dyes and Pigments, 2017, 136, 697-706.
  6. Kunaseth, M.; Poldorn, P.; Junkeaw, A.; Meeprasert, J.; Rungnim, C.; Namuangruk, S.; Kungwan,N.; Inntam, C.; Jungsuttiwong. S. DFT study of volatile organic compounds adsorption on transition metal deposited graphene Applied Surface Science, 2017, 396, 1712–1718.
  7. Insuwan, W.; Rangsriwatananon, K.; Meeprasert, J.; Namuangruk, S.; Surakhot, Y.; Kungwan,N.; Jungsuttiwong, S. Combined Experimental and Theoretical Investigation on Fluorescence Resonance Energy Transfer of Dye Loaded on LTL Zeolite, Microporous and Mesoporous Materials, 2017, 241, 372-382.
  8. Surakhot, Y.; Laszlo, V.; Chitpakdee, C.; Promarak, V.; Sudyoadsuk, T.; Kungwan, N.; Kowalczyk, T.; Irle, S.; Jungsuttiwong, S. Theoretical Rationalization for Reduced Charge Recombination in Bulky Carbazole-Based Sensitizers in Solar Cells, Journal of Computational Chemistry, 2017, 38 (12), 901–909.
  9. Chitpakdee, C.; Jungsuttiwong, S.; Sudyoadsuk, T.; Promarak, V.; Kungwan, N.; Namuangruk, S. Modulation of π-spacer of carbazole-carbazole based organic dyes toward high efficient dye-sensitized solar cells, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2017, 174, 7–16.
  10. Jiang, Y.; Cabanetos, C.; Jungsuttiwong, S.; Alberga, D.; Adamo, C.; Roncali, J. Effects of Anthryl Groups on the Charge Transport and Photovoltaic Properties of Small Triarylamine-Based Donor-Acceptor Molecules: A Joint Experimental and Theoretical Study, ChemistrySelect, 2017, 2, 6296-6303.
  11. Prachumrak, N.; Sudyoadsuk, T.; Thangthong, A.; Nalaoh, P.; Jungsuttiwong, S.; Daengngern, R.; Namuangruk, S.; Pattanasattayavong, P.; Promarak, V, Improvement of D-pi-A organic dye-based dye-sensitized solar cell performance by simple triphenylamine donor substitutions on the pi-linker of the dye Materials Chemistry Frontiers, 2017, 1, 1059-1072.

2016

  1. Jiang, Y.; Cabanetos, C.; Allain, M.; Jungsuttiwong, S.; Roncali, J. Manipulation of the electronic and photovoltaic properties of materials based on small push-pull molecules by substitution of the arylamine donor block by aliphatic groups, Organic Electronics, 2016, 37, 294-304.
  2. Kunaseth, M.; Mudchimo, T.; Namuangruk, S.; Kungwan, N.; Promarak, V.; Jungsuttiwong, S. A DFT study of arsine adsorption on palladium doped graphene:Effects of palladium cluster size, Applied Surface Science, 2016, 367, 552–558.
  3. Jungsuttiwong, S.; Wongnongwa, Y.; Namuangruk, S.; Kungwan, N.; Promarak, V.; Kunaseth, M. Density functional theory study of elemental mercury adsorption on boron doped graphene surface decorated by transition metals, Applied Surface Science, 2016, 362, 140-145.
  4. Rattanawan, R.; Promarak, V.; Sudyoadsuk, T.; Namuangruk, S.; Kungwan, N.; Yuan, S.; Jungsuttiwong, S.; Theoretical design of coumarin derivatives incorporating auxiliary acceptor with D--A--A configuration for dye-sensitized solar cells, Journal of Photochemistry and Photobiology A: Chemistry, 2016, 322, 16–26.
  5. Muenmart, D.; Prachumrak, N.; Tarsang, R. ; Pattanasattayavong, P.; Namuangruk, S.; Jungsuttiwong, S.; Sudyoadsuk, T.; Promarak, V. New D-D-pi-A type organic dyes having carbazol-N-yl phenothiazine moiety as a donor (D-D) unit for efficient dye-sensitized solar cells: experimental and theoretical studies, RSC ADVANCES, 2016, 6, 38481-38493.
  6. Demeter, D.; Melchiorre, F.; Biagini, P.; Jungsuttiwong,;S.; Po, R.; Roncali, J. Tetrahedron Letters, 2016, 57, 4815-4820.
  7. Tarsang, R.; Jungsuttiwong, S.; Vao-soongnern, V. Computational and Theoretical Chemistry, 2016, 1098, 31-40.
  8. Kaewpuang, T.; Prachumrak, N.; Namuangruk, S.; Jungsuttiwong, S.; Sudyoadsuk, T.; Pattanasattayavong, P.; Promarak, V. European Journal of Organic Chemistry, 2016, 2528-2538.
  9. Namuangruk, S.; Jungsuttiwong, S.; Kungwan, N.; Promarak, V.; Sudyoadsuk, T.; Jansang, B.; Ehara, M. Coumarin-based donor--acceptor organic dyes for a dye-sensitized solar cell: photophysical properties and electron injection mechanism Theoretical Chemistry Accounts, 2016, 135, Article Number: 14.

2015

  1. Demeter, D.; Roncali, J.; Jungsuttiwong, S.; Melchiorre, F.; Biagini, P.; Po, R. Linearly pi-conjugated oligothiophenes as simple metal-free sensitizers for dye-sensitized solar cells, Journal of Materials Chemistry C, 2015, 3, 29, 7756-7761.
  2. Diac, A; Demeter, D.; Jungsuttiwong, S.; Grosu, I.; Roncali, J. ADDA and ADADA systems based on triphenylamine as molecular donors for organic photovoltaics, Tetrahedron Letters, 2015, 56, 4607–4612.
  3. Sangchart, T.; Niroram, Arunroj.; Kaewpuang, T.; Prachumrak, N.; Namuangruk, S.; Sudyoadsuk, T.; Keawin, T.; Saengsuwan, S.; Jungsuttiwong, S.; Maensiri, S.; Kungwan, N.; Promarak, V. Synthesis, physical and electroluminescence properties of 3,6-dipyrenylcarbazole end capped oligofluorenes, RSC Advances, 2015, 5, 26569–26579.
  4. Keawin, T.; Sooksai, C.; Prachumrak, N.; Kaewpuang, T.; Muenmart, D.; Namuangruk, S.; Jungsuttiwong, S.; Sudyoadsuk, T.; Promarak, V. Oligoarylenes end-capped with carbazol-N-yl-carbazole as color tunable light-emitting and hole-transporting materials for solution-processed OLEDs, RSC Advances, 2015, 5, 16422-16432.
  5. Keawin, T.; Prachumrak, N.; Namuangruk, S.; Pansay, S.; Kungwan, N.; Maensiri, S.; Jungsuttiwong, S.; Sudyoadsuk, T. Promarak, V. Efficient bifunctional materials based on pyrene- and triphenylamine-functionalized dendrimers for electroluminescent devices. RSC ADVANCES, 2015, 5, 73481-73489.
  6. Ngaojampa, C.; Namuangruk, S.; Surakhot, Y.; Promarak, V.; Jungsuttiwong, S.; Kungwan, N.; Influence of phenyl-attached substituents on the vibrational and electronic spectra of meso-tetraphenylporphyrin: A DFT study, Computational and Theoretical Chemistry, 2015, 1062, 1–10.
  7. Surakhot, Y.; Rattanawan, R.; Ronyhut, K.; Mangsachart, P.; Sudyoadsuk, T.; Promarak, V.; Namuangruk, S.; Kungwan, N.; Jungsuttiwong, S., The number density effect of N-substituted dyes on the TiO2 surface in dye sensitized solar cells: a theoretical study, RSC Advances, 2015, 5, 11549.
  8. Kotchapradist, P.; Prachumrak, Narid.; Sunonnam, Thitiya.; Tarsang, R.; Namuangruk, S.; Sudyoadsuk, T.; Keawin, T.; Jungsuttiwong, S.; Promarak, V. N-coumarin derivatives as hole-transporting emitters for high efficiency solution-processed pure green electroluminescent devices, Dyes and Pigments, 2015, 112, 227-235.
  9. Kotchapradist, P.; Prachumrak, Narid.; Sunonnam, Thitiya.; Namuangruk, S.; Sudyoadsuk, T.; Keawin, T.; Jungsuttiwong, S.; Promarak, V. Synthesis, Characterisation, and Electroluminescence Properties of N-Coumarin Derivatives Containing Peripheral Triphenylamine, European Journal of Organic Chemistry, 2015, 3, 496-505
  10. Insuwan, W.; Jungsuttiwong, S.; Rangsriwatananon, K. Host–guest composite materials of dyes loaded zeolite LTL for antenna applications, Journal of Luminescence, 2015, 161, 31-36.
  11. Chitpakdee, C.; Namuangruk, S.; Suttisintong, K.; Jungsuttiwong, S.; Keawin, T.; Sudyoadsuk, T.; Sirithip, K.; Promarak, V.; Kungwan, N. Effects of pi-linker, anchoring group and capped carbazole at meso-substituted zinc-porphyrins on conversion efficiency of DSSCs, Dyes and Pigments, 2015, 118, 64-75.
  12. Thangthong, A.; Prachumrak, N.; Sudyoadsuk, T.; Namuangruk, S.; Keawin, T.; Jungsuttiwong, S.; Kungwan, N.; Promarak, V. Multi-triphenylamine-functionalized dithienylbenzothiadiazoles as hole-transporting non-doped red emitters for efficient simple solution processed pure red organic light-emitting diodes, Organic Electronics, 2015, 21, 117-125.
  13. Sirithip, K.; Prachumrak, N.; Rattanawan, R.; Keawin, T.; Sudyoadsuk, T.; Namuangruk, S.; Jungsuttiwong, S.; Promarak, V. Zinc-Porphyrin Dyes with Different meso-Aryl Substituents for Dye-Sensitized Solar Cells: Experimental and Theoretical Studies, Chemistry-An Asian Journal, 2015, 10, 882-893.
  14. Tarsang, R.; Promarak, V.; Sudyoadsuk, T.; Namuangruk, S.; Kungwan, N.; Khongpracha, P.; Jungsuttiwong, S. Triple bond-modified anthracene sensitizers for dye-sensitized solar cells: a computational study, RSC Advances, 2015, 5, 38130-38140.
  15. Thangthong, A.; Prachumrak, N.; Saengsuwan, S.; Namuangruk, S.; Keawin, T.; Jungsuttiwong, S.; Sudyoadsuk, T.; Promarak, V. Multi-triphenylamine-substituted bis(thiophenyl) benzothiadiazoles as highly efficient solution-processed non-doped red light-emitters for OLEDs, Journal of Materials Chemistry C. 2015, 3, 3081-3086.

2014

  1. Tarsang, R.; Promarak, V.; Sudyoadsuk, T.; Namuangruk, S.; Jungsuttiwong, S., Tuning the Electron Donating Ability in the Triphenylamine-Based D-t-A Architecture for Highly Efficient Dye-Sensitized Solar Cells, Journal of Photochemistry and Photobiology A: Chemistry, 2014, 273, 8-16.
  2. Chitpakdee, C.; Namuangruk, S.; Khongpracha, P.; Jungsuttiwong, S.; Tarsang, R.; Sudyoadsuk, T.; Promarak, V., Theoretical studies on electronic structures and photophysical properties of anthracene derivatives as hole-transporting materials for OLEDs, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2014, 125, 36-45.
  3. Meeprasert, J.; Kungwan, N.; Jungsuttiwong, S.; Namuangruk, S.; Location and reactivity of extra-framework cation in the alkali exchanged LTL zeolites: A periodic density functional study, Microporous and Mesoporous Materials, 2014, 195, 227-239.
  4. Khanasa, T.; Prachumrak, N.; Kochapradist, P.; Namuangruk, S.; Keawin, T.; Jungsuttiwong, S.; Sudyoadsuk, T,; Promarak, V., The design, synthesis, and characterization of D-π-A-π-A type organic dyes as sensitizers for dye-sensitized solar cells (DSSCs), Tetrahedron Letters, 2014, 55, 3244-3248.
  5. Namuangruk, S.; Sirithip, K.; Rattanatwan, R.; Keawin, T.; Kungwan, N.; Sudyodsuk, T.; Promarak, V.; Jungsuttiwong, S., Theoretical Investigation of the Charge-Transfer Properties in Different Meso-linked Zinc Porphyrin for Highly Efficient Dye-Sensitized Solar Cells, Dalton Transactions, 2014, 43 , 9166–9176.
  6. Prachumrak, N.; Potjanasopa, S.; Rattanawan, R.; Namuangruk, S.; Jungsuttiwong, S.; Keawin, T.; Sudyoadsuk, T,; Promarak, V., Coumarin-cored carbazole dendrimers as solution-processed non-doped green emitters for electroluminescent devices, Tetrahedron, 2014, 70(36), 6249-6257.
  7. Sudyoadsuk, T.; Moonsin, P.; Prachumrak, N.; Namuangruk, S.; Jungsuttiwong, S.; Keawin, T.; Promarak, V., Carbazole Dendrimers Containing Oligoarylfluorene Cores As Solution-Processed Hole-Transporting Non-Doped Emitters for Efficient Pure Red, Green, Blue and White Organic Light-Emitting Diodes, Polymer Chemistry, 2014, 5, 3982-3993.
  8. Moonsin, P.; Prachumrak, N.; Namuangruk, S.; Jungsuttiwong, S.; Keawin, T.; Sudyoadsuk, T.; Promarak, V., Bifunctional oligofluorene-cored carbazole dendrimers as solution-processed blue emitters and hole transporters for electroluminescent devices, Journal of Materials Chemistry C, 2014, 2 (28), 5540 – 5552.
  9. Thongkasee, P.; Thangthong, A.; Janthasing, N.; Sudyoadsuk, T.; Namuangruk, S.; Keawin, T.; Jungsuttiwong, S.; Promarak, V., Carbazole-Dendrimer-Based Donor-p–Acceptor Type Organic Dyes for Dye-Sensitized Solar Cells: Effect of the Size of the Carbazole Dendritic Donor, ACS Applied Materials & Interfaces, 2014, 6 (11), 8212–8222.
  10. Prachumrak, N.; Pojanasopa, S.; Tarsang, R.; Namuangruk, S.; Jungsuttiwong, S.; Keawin, T.; Sudyoadsuk, T.; Promarak, V., Synthesis and characterization of carbazole dendronized coumarin derivatives as solution-processed non-doped emitters and hole-transporters for electroluminescent devices, New Journal of Chemistry, 2014, 38 (7), 3282 – 3294.
  11. Insuwan, W.; Rangsriwatananon, K.; Meeprasert, J.; Namuangruk, S.; Surakhot, Y.; Kungwan, N.; Jungsuttiwong, S., Combined experimental and theoretical investigation on photophysical properties of trans-azobenzene confined in LTL zeolite: Effect of cis-isomer forming, Microporous and Mesoporous Materials, 2014, 197 348–357.
  12. Tarsang, R.; Promarak, V.; Sudyoadsuk, T.; Namuangruk, S.; Kungwan, N.; Jungsuttiwong, S., Modification on D-A-π-A Configuration toward High-Performance Starburst Triphenylamine-Based Sensitizer for Dye Sensitized Solar Cells: A Theoretical Investigation, ChemPhysChem, 2014, 15, 3809 – 3818.
  13. Kungwan, N.; Khongpracha, P.; Namuangruk, S.; Meeprasert, J.; Chitpakdee, C.; Jungsuttiwong, S.; Promarak, V., Theoretical study of linker-type effect in carbazole-carbazole-based dyes on performances of dye-sensitized solar cells, Theoretical Chemistry Accounts, 2014, 133, 1523.
  14. Namuangruk, S.; Meeprasert, J.; Jungsuttiwong, S.; Promarak, V.; Kungwan, N., Organic sensitizers with modified di (thiophen‑2‑yl)phenylamine donor units for dye-sensitized solar cells: a computational study. Theoretical Chemistry Accounts, 2014, 133, 1534.

2013

  1. Piansawan, T., Kungwan, N., and Jungsuttiwong, S. Application of the reaction class transition state theory to the kinetics of hydrogen abstraction reactions of alkanes by atomic chlorine, Computational and Theoretical Chemistry, 2013, 1011, 65–74.
  2. Meeprasert, J., Jungsuttiwong, S., Truong, T. N. and Namuangruk, S. Effects of Amine Organic Groups as Lattice in ZSM-5 on the Hydrolysis of Dimethyl Ether, Journal of Molecular Graphics and Modelling, 2013, 43, 31-40.
  3. Meeprasert, J., Jungsuttiwong, S., and Namuangruk, S. Location and Acidity of Brønsted acid sites in Isomorphously Substituted LTL Zeolite: A Periodic Density Functional Study, Microporous and Mesoporous Materials, 2013, 175, 99–106.
  4. Prachumrak, N.; Pojanasopa, S.; Namuangruk, S.; Kaewin, T.; Jungsuttiwong, S.; Sudyoadsuk, T.; Promarak, V., Novel Bis[5-(fluoren-2-yl)thiophen-2-yl]benzothiadiazole End-Capped with Carbazole Dendrons as Highly Efficient Solution-Processed Nondoped Red Emitters for Organic Light-Emitting Diodes, ACS Applied Materials & Interfaces, 2013, 5(17), 8694–8703.
  5. Prachumrak, N.; Pansay, S.; Namuangruk, S.; Keawin, T.; Jungsuttiwong, S.; Sudyoadsuk, T.; Promarak, V., Synthesis and Characterization of Carb¬azole Dendrimers as Solution-Processed High TgAmorphous Hole-Transporting Materials for Electroluminescent Devices, European Journal of Organic Chemistry, 2013, 29, 6619-6623.
  6. Sudyoadsuk, T.; Khunchalee, J.; Pansay, S.; Tongkasee, P.; Morada, S.; Kaewin, T.; Jungsuttiwong, S.; Promarak, V., An organic dye using N-dodecyl-3-(3,6-di-tert-butylcarbazol-N-yl)carbazol-6-yl as a donor moiety for efficient dye-sensitized solar cells, Tetrahedron Letters, 2013, 54, 4903-4907.
  7. Khanasa, T.; Prachumrak, N.; Rattanawan, R.; Jungsuttiwong, S.; Keawin, T.; Sudyoadsuk, T.; Tuntulani, T.; Promarak, V., Bis(carbazol-9-ylphenyl)aniline End-Capped Oligoarylenes as Solution-Processed Nondoped Emitters for Full-Emission Color Tuning Organic Light-Emitting Diodes, The Journal of Organic Chemistry 2013, 78 (13), 6702–6713.
  8. Kotchapradist, P.; Prachumrak, N.; Tarsang, R.; Jungsuttiwong, S.; Keawin, T.; Sudyoadsuk, T.; Promarak, V., Pyrene-functionalized carbazole derivatives as non-dope blue emitters for highly efficient blue organic light-emitting diodes, Journal of Materials Chemistry C 2013, 1, 4916-4924.
  9. Moonsin, P.; Prachumrak, N.; Namuangruk, S.; Jungsuttiwong, S.; Keawin, T.; Sudyoadsuk, T.; Promarak, V., Novel bis(fluorenyl)benzothiadiazole-cored carbazole dendrimers as highly efficient solution-processed non-doped green emitters for organic light-emitting diodes, Chemical Communications 2013, 49 (57), 6388-6390.
  10. Sudyoadsuk, T.; Pansay, S.; Morada, S.; Rattanawan, R.; Namuangruk, S.; Kaewin, T.; Jungsuttiwong, S.; Promarak, V., Synthesis and Characterization of D–D–p–A-Type Organic Dyes Bearing Carbazole–Carbazole as a Donor Moiety (D–D) for Efficient Dye-Sensitized Solar Cells, European Journal of Organic Chemistry 2013, 23, 5051-5053.
  11. Kochapradist, P.; Prachumrak, N.; Tarsang, R.; Keawin, T.; Jungsuttiwong, S.; Sudyoadsuk, T.; Promarak, V., Multi-triphenylamine-substituted carbazoles: synthesis, characterization, properties and applications as hole-transporting materials, Tetrahedron Letters, 2013, 54, 3683–3687.
  12. Prachumrak, N.; Namuangruk, S.; Keawin, T.; Jungsuttiwong, S.; Sudyoadsuk, T.; Promarak, V., Synthesis and Characterization of 9-(Fluorene-2-yl)anthracene Derivatives as Efficient Non-Doped Blue Emitters for Organic Light-Emitting Diodes, European Journal of Organic Chemistry, 2013, 2013, 18, 3825-3834.
  13. Sirithip, K.; Morada, S.; Namuangruk, S.; Keawin, T.; Jungsuttiwong, S.; Sudyoadsuk, T.; Promarak, V., Synthesis and characterization of β-pyrrolic functionalized porphyrins as sensitizers for dye-sensitized solar cells, Tetrahedron Letters, 2013, 54, 2435-2439.
  14. Khanasa T., Prachumrak, N., Rattanawan R., Jungsuttiwong S., Kaewin T., Sudyoadsuk T., Tuntulani T., Promarak V. Efficient Solution Processed Non-doped Red Emitter Based on Carbazole-triphenylamine End-capped Di(thiophen-2-yl)benzothiadiazole for Pure Red Organic Light-emitting Diode, Chemical Communications, 2013, 49, 3401-3403.
  15. Khanasa T., Jantasing N., Morada S., Leesakul N., Tarsang R., Namuangruk S., Kaewin T., Jungsuttiwong S., Sudyoadsuk T., Promarak V. Synthesis and Characterization of 2D-D-p-A-Type Organic Dyes Bearing Bis(3,6-di-tert-butylcarbazol-9-ylphenyl)aniline as Donor Moiety for Dye-Sensitized Solar Cells, European Journal of Organic Chemistry, 2013, 13, 2608-2620.
  16. Jungsuttiwong, S.; Tarsang, R.; Sudyoadsuk, T.; Promarak, V.; Khongpracha, P.; Namuangruk, S. Theoretical Study on Novel Double Donor-based Dyes used in High Efficient Dye-sensitized Solar Cells: The Application of TDDFT Study to The Electron Injection Process, Organic Electronics, 2013, 14(3), 711-722.

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